Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health
Reference5 articles.
1. Intravenous iron among cystic fibrosis patients;Hoo;J Cyst Fibros,2012
2. Increased iron and ferritin content of sputum from patients with cystic fibrosis or chronic bronchitis;Stites;Chest,1998
3. Iron deficiency in cystic fibrosis: relationship to lung disease severity and chronic Pseudomonas aeruginosa infection;Reid;Chest,2002
4. Iron-binding compounds impair Pseudomonas aeruginosa biofilm formation, especially under anaerobic conditions;O'May;J Med Microbiol,2009
5. Improved differential diagnosis of anemia of chronic disease and iron deficiency anemia: a prospective multicenter evaluation of soluble transferrin receptor and the sTfR/log ferritin index;Skikne;Am J Hematol,2011
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Iron Deficiency in Cystic Fibrosis: A Cross-Sectional Single-Centre Study in a Referral Adult Centre;Nutrients;2022-02-05
2. Authors’ response: Letter to the Editor ‘Anaemia and iron deficiency in relation to fatigue in cystic fibrosis’;Journal of Cystic Fibrosis;2019-01
3. Serum Hepcidin Level as a Marker of Iron Status in Children with Cystic Fibrosis;Mediators of Inflammation;2018-07-02
4. Regarding the article entitled “Iron supplementation does not worsen respiratory health or alter the sputum microbiome in cystic fibrosis”;Journal of Cystic Fibrosis;2015-01
5. The value of soluble transferrin receptor and hepcidin in the assessment of iron status in children with cystic fibrosis;Journal of Cystic Fibrosis;2014-12
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